Innomed, Inc.

FDA UDI

Class I (US FDA UDI)

by Innomed, Inc.

Identity

Trade Name: Innomed, Inc. FDA UDI
Generic Name: Cannula clamp FDA UDI
Device Name: McMaster Medullary Canal Aspirator Tube FDA UDI
Model / Reference: 8075-01 FDA UDI
Description: McMaster Medullary Canal Aspirator Tube FDA UDI

Identifiers

Catalog Number: 8075-01 FDA UDI
Primary DI / UDI-DI: 00840277124937 FDA UDI
FDA Product Code: FKC FDA UDI
GMDN Term: Cannula clamp FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 876.5540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Cannula clamp

Innomed, Inc. by Innomed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Innomed, Inc. — Innomed, Inc. · Class I
Innomed, Inc. — Innomed, Inc. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Innomed, Inc.

Sources (1)

FDA UDI b86c4c17-d8c4-4ccf-a2d3-4c07a71107b1 34 fields · synced Jun 8, 2026